Clinical Trials Research Associate I

Montefiore Health System; New York (NY); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

Montefiore Health System seeks a Cancer Clinical Trials CRC I to support the research team under supervision. You will handle primary data collection, manage patient information, and assist with protocol related samples while ensuring compliance with Good Clinical Practice.

You will participate in recruitment activities, obtain informed consent for studies, and help organize data submission, registrations, and source documents across multiple studies at the site in New York.

Qualifications

• Bachelor's degree required.
• Masters degree preferred.
• ACRP or SOCRA certification preferred.
• Life science/public health degree preferred.
• Medical degree preferred.

Responsabilités

• Collects and records study data; inputs into database.
• Assists in recruitment activities and screening.
• Maintains source documents and subject files per procedures.
• Coordinates SFV, SIVs and monitor scheduling, including remote access.

Connaissances

Data collection

Data entry

Study coordination

Informed consent

Source documents

Formation

Bachelor's degree

Master's degree

ACRP certification

SOCRA certification

Life science/public health degree

Medical degree

Description du poste

Montefiore Health System seeks a Cancer Clinical Trials CRC I to support the research team under supervision. You will handle primary data collection, manage patient information, and assist with protocol related samples while ensuring compliance with Good Clinical Practice.

You will participate in recruitment activities, obtain informed consent for studies, and help organize data submission, registrations, and source documents across multiple studies at the site in New York.